Genetic Test Details

Neuromuscular Channelopathies Panel

Test Information

Title
Neuromuscular Channelopathies Panel
Lab
Lab
Category
Neurogenetics
Sub Category
Neuromuscular Disease
Gene/Platform/Region List
ATP1A2, CACNA1A, CACNA1S, CLCN1, KCNA1, KCNE3, KCNJ2, SCN4A, SLC12A3
Test type
Gene Panel
Samples Accepted
Blood , DNA
Indications
Carrier Cascade Testing , Diagnosis
Test Methodology
Sequencing
Disease/Condition
Neuromuscular Channelopathies, myotonia congenita, paramyotonia congenita, hyperkalemic periodic paralysis, hypokalemic periodic paralysis, Andersen-Tawil syndrome, potassium-aggravated myotonia

Last Updated: September 05, 2025